Term Name: | autosomal recessive nonsyndromic deafness 1B |
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Synonyms: | autosomal recessive deafness 1B, DFNB1B |
Definition: | An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and has_material_basis_in mutation in the GJB6 gene on chromosome 13q12. |
Ontology: | Human Disease [DOID:0110476] ( DOID:0110476 ) |